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1. 569-80-2
2. 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxychromen-4-one
3. 5,4'-dihydroxy-3,6,7-trimethoxyflavone
4. Chembl165509
5. 5,4'-dihydroxy-3,6,7-trimethoxyflavone; 6-hydroxykaempferol 3,6,7-trimethyl Ether
6. 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxy-chromen-4-one
7. Schembl2217068
8. Dtxsid00205437
9. Bdbm50338973
10. Lmpk12112874
11. Nsc659549
12. Zinc14644952
13. 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxy-4h-1-benzopyran-4-one
14. Akos032948446
15. Nsc-659549
16. Xp161712
17. 3,6,7-trimethyl-6-hydroxykaempferol
18. 5,4''-dihydroxy-3,6,7-trimethoxyflavanone
19. 5-hydroxy-2-(4-hydroxy-phenyl)-3,6,7-trimethoxy-chromen-4-one
20. 4h-1-benzopyran-4-one, 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxy-
21. 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxy-4h-chromen-4-one #
22. 2-(4-hydroxyphenyl)-3,6,7-trimethoxy-5-hydroxy-4h-1-benzopyran-4-one (penduletin)
| Molecular Weight | 344.3 g/mol |
|---|---|
| Molecular Formula | C18H16O7 |
| XLogP3 | 3.1 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | 344.08960285 g/mol |
| Monoisotopic Mass | 344.08960285 g/mol |
| Topological Polar Surface Area | 94.4 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 524 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Penduletin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penduletin, including repackagers and relabelers. The FDA regulates Penduletin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penduletin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Penduletin supplier is an individual or a company that provides Penduletin active pharmaceutical ingredient (API) or Penduletin finished formulations upon request. The Penduletin suppliers may include Penduletin API manufacturers, exporters, distributors and traders.
Penduletin Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Penduletin GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Penduletin GMP manufacturer or Penduletin GMP API supplier for your needs.
A Penduletin CoA (Certificate of Analysis) is a formal document that attests to Penduletin's compliance with Penduletin specifications and serves as a tool for batch-level quality control.
Penduletin CoA mostly includes findings from lab analyses of a specific batch. For each Penduletin CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Penduletin may be tested according to a variety of international standards, such as European Pharmacopoeia (Penduletin EP), Penduletin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Penduletin USP).
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